Variant report

Variant	rs10248432
Chromosome Location	chr7:14383801-14383802
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10085673	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10270714	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17167967	1.00[EUR][1000 genomes]
rs6461084	1.00[EUR][1000 genomes]
rs6944496	1.00[EUR][1000 genomes]
rs740398	1.00[EUR][1000 genomes]
rs7788063	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3347566	chr7:14382677-14384825	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14383000-14384000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:14383200-14390800	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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